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rs118203904

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118203904(A;G)
Make rs118203904(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position232790817
GeneGIGYF2
is asnp
is mentioned by
dbSNPrs118203904
ebirs118203904
HLIrs118203904
Exacrs118203904
Varsomers118203904
Maprs118203904
PheGenIrs118203904
hapmaprs118203904
1000 genomesrs118203904
hgdprs118203904
ensemblrs118203904
gopubmedrs118203904
geneviewrs118203904
scholarrs118203904
googlers118203904
pharmgkbrs118203904
gwascentralrs118203904
openSNPrs118203904
23andMers118203904
23andMe allrs118203904
SNP Nexus

SNPshotrs118203904
SNPdbers118203904
MSV3drs118203904
GWAS Ctlgrs118203904
GMAF0.0004591
Max Magnitude0
OMIM612003
Desc
Variant0004
Relatedalso
ClinVar
Risk rs118203904(G;G)
Alt rs118203904(G;G)
Reference rs118203904(A;A)
Significance Other
Disease Parkinson disease 11
Variation info
Gene GIGYF2
CLNDBN Parkinson disease 11
Reversed 0
HGVS NC_000002.11:g.233655527A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000792.4,